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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1032515생성일: 2026년 10월 25일

(4-Benzyloxy-3-nitrophenyl)acetonitrile → (3-Amino-4-benzyloxyphenyl)acetonitrile

https://huagongshe.com/reaction/1032515

반응식

참여 물질

역할이름HCID투입량
반응물(4-Benzyloxy-3-nitrophenyl)acetonitrileHCID 13629303—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
용매MethanolHCID 887—
생성물(3-Amino-4-benzyloxyphenyl)acetonitrileHCID 2216598676.7%

반응 단계

In the presence of Raney nickel, 53.6 g of (4-benzyloxy-3-nitrophenyl)acetonitrile in 1.2 1 of methanol is hydrogenated until 12.2 1 of hydrogen has been absorbed. The crude product obtained after removing the catalyst by filtration and after evaporation is purified by chromatography on silica gel with cyclohexane/ethyl acetate (1:1), thus obtaining 36.5 g of (3-amino-4-benzyloxyphenyl)acetonitrile as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04958026
출처 데이터셋uspto-grants-1990_09
ORD IDord-d58da132a73e4c47ac43e5600e2d7cee
출처 메모uspto-grants-1990_09